Prabowo A S, van Scheppingen J, Iyer A M, Anink J J, Spliet W G M, van Rijen P C, Schouten-van Meeteren A Y N, Aronica E
Department of (Neuro)Pathology, Academic Medical Center, University of Amsterdam, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.
Department of Pathology, Rudolf Magnus Institute for Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
J Neuroinflammation. 2015 May 20;12:97. doi: 10.1186/s12974-015-0315-7.
miR21, miR146, and miR155 represent a trio of microRNAs which has been shown to play a key role in the regulation of immune and inflammatory responses. In the present study, we investigated the differential expression and clinical significance of these three miRNAs in glioneuronal tumors (gangliogliomas, GGs) which are characterized by prominent activation of the innate immune response.
The expression levels of miR21, miR146, and miR155 were evaluated using Taqman PCR in 34 GGs, including 15 cases with sufficient amount of perilesional cortex. Their expression was correlated with the tumor features and the clinical history of epilepsy. In addition, in situ hybridization was used to evaluate their cellular distribution in both tumor and peritumoral cortex.
Increased expression of miR146a was observed in both tumor and peritumoral cortex compared to control samples. miR146a was detected in both neuronal and astroglial cells. Tumor and peritumoral miR146a expression was negatively correlated with frequency of seizures and the density of activated microglial cells. Neuronal and astroglial expression was observed for both miR21 and miR155 with increased expression of miR21 within the tumor and miR155 in the peritumoral region. Negative correlations were observed between the miRNA levels and the expression of putative targets within the astroglial component of the tumor.
We report a differential regulation of three miRNAs, known to be related to inflammation, in both tumor and peritumoral cortex of patients with GG. Moreover, our findings suggest a functional relationship between miR146a expression and epilepsy, either directly in epileptogenesis or as modulation of seizure activity.
miR21、miR146和miR155是一组微小RNA,已被证明在免疫和炎症反应调节中起关键作用。在本研究中,我们调查了这三种微小RNA在以先天性免疫反应显著激活为特征的神经胶质神经元肿瘤(神经节胶质瘤,GGs)中的差异表达及其临床意义。
使用Taqman PCR评估34例GGs中miR21、miR146和miR155的表达水平,其中15例有足够量的瘤周皮质。它们的表达与肿瘤特征和癫痫临床病史相关。此外,采用原位杂交评估它们在肿瘤和瘤周皮质中的细胞分布。
与对照样本相比,在肿瘤和瘤周皮质中均观察到miR146a表达增加。在神经元和星形胶质细胞中均检测到miR146a。肿瘤和瘤周miR146a表达与癫痫发作频率和活化小胶质细胞密度呈负相关。在肿瘤内miR21表达增加,在瘤周区域miR155表达增加,在miR21和miR155的神经元和星形胶质细胞中均观察到这种情况。在肿瘤星形胶质细胞成分中,微小RNA水平与假定靶标的表达之间存在负相关。
我们报告了在GG患者的肿瘤和瘤周皮质中,三种已知与炎症相关的微小RNA存在差异调节。此外,我们的研究结果表明miR146a表达与癫痫之间存在功能关系,可能直接参与癫痫发生或调节癫痫发作活动。